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先天性内脏反位合并永存左上腔静脉时冠状静脉窦口闭锁的外科修复术

Surgical repair of coronary sinus orifice atresia with persistent left superior vena cava in heterotaxia.

作者信息

Takabayashi Shin, Shimpo Hideto, Yokoyama Kazuto

机构信息

Department of Thoracic and Cardiovascular Surgery, Mie University Graduate School of Medicine, 2-174 Edobashi, Tsu, Mie 514-8507, Japan.

出版信息

Gen Thorac Cardiovasc Surg. 2007 May;55(5):197-9. doi: 10.1007/s11748-007-0104-z.

Abstract

A 6-month-old boy was diagnosed with coronary sinus orifice atresia, double-outlet right ventricle, complete atrioventricular septal defect, pulmonary stenosis, and moderate common atrioventricular valve regurgitation associated with heterotaxy syndrome. Cardiac venous flow drained through a persistent left superior vena cava. We decided to perform coronary sinus orifice unroofing through the right atrium under a guide using a bougie. The persistent left superior vena cava was divided. Bidirectional Glenn anastomosis and edge-to-edge common atrioventricular valve repair were concomitantly performed. After a 1-year follow-up period, the patient is alive and well without any ischemic event.

摘要

一名6个月大的男婴被诊断为冠状静脉窦口闭锁、右心室双出口、完全性房室间隔缺损、肺动脉狭窄以及与内脏异位综合征相关的中度共同房室瓣反流。心脏静脉血流经持续存在的左上腔静脉引流。我们决定在导丝引导下经右心房进行冠状静脉窦口开窗术。将持续存在的左上腔静脉离断。同时进行双向格林吻合术和共同房室瓣的缘对缘修复。经过1年的随访期,患者存活且状况良好,未发生任何缺血事件。

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